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疟原虫维生素 B 代谢作为药物靶点的来源。

Vitamin B metabolism in Plasmodium falciparum as a source of drug targets.

机构信息

Department of Biochemistry, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.

出版信息

Trends Parasitol. 2010 Jan;26(1):35-43. doi: 10.1016/j.pt.2009.10.006. Epub 2009 Nov 24.

Abstract

The malaria parasite Plasmodium falciparum depends primarily on nutrient sources from its human host. Most compounds, such as glucose, purines, amino acids, as well as cofactors and vitamins, are abundantly available in the host cell, and can be readily salvaged by the parasite. However, in some cases the parasite can also synthesize cofactors de novo in reactions that appear to be essential. Importantly, the three biosynthetic pathways that produce vitamins B(1), B(6) and B(9) are absent from the host, but are well established in P. falciparum. This review summarizes and updates the current knowledge of vitamin B de novo synthesis and salvage in P. falciparum and focuses on their potential as targets for drug intervention.

摘要

疟原虫恶性疟原虫主要依赖于来自其人类宿主的营养来源。大多数化合物,如葡萄糖、嘌呤、氨基酸以及辅助因子和维生素,在宿主细胞中大量存在,并且可以被寄生虫轻易回收利用。然而,在某些情况下,寄生虫也可以通过似乎必不可少的反应从头合成辅助因子。重要的是,宿主中不存在产生维生素 B(1)、B(6)和 B(9)的三种生物合成途径,但在恶性疟原虫中已得到很好的确立。本文综述了恶性疟原虫中从头合成和回收利用维生素 B 的最新知识,并重点探讨了它们作为药物干预靶点的潜力。

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